|Publication number||US4102806 A|
|Application number||US 05/715,192|
|Publication date||Jul 25, 1978|
|Filing date||Aug 17, 1976|
|Priority date||Aug 18, 1975|
|Also published as||CA1071935A, CA1071935A1|
|Publication number||05715192, 715192, US 4102806 A, US 4102806A, US-A-4102806, US4102806 A, US4102806A|
|Inventors||Sadao Kondo, Hidehiko Nakano|
|Original Assignee||Takeda Chemical Industries, Ltd.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (9), Referenced by (91), Classifications (49)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This invention relates to a method comprising encapsulating a particulate core material with an oleaginous material in an organic solvent.
Among the encapsulating methods employing oleaginous materials by way of shell-forming component is the fusing method which comprises heating an oleaginous material until it is fused and coating a core material with the resultant melt in a suitable vehicle, another known method comprising the steps of dissolving an oleaginous material in a solvent, dispersing a particulate core material in the solution, and removing the solvent in a suitable manner so as to leave the individual cores coated with said oleaginous material, the latter method being known as the organic solvent method. The fusing method has two versions, one comprising the use of a gaseous phase as the vehicle and the other employing a liquid phase as the vehicle. While both processes are fully practical for the encapsulation of some core materials, the following disadvantages are unavoidable. Thus, where a gaseous phase is used as the vehicle, large-scale spray-chilling equipment must be provided. In the process employing a liquid phase as the vehicle, particularly where said phase is water, for instance, a water-soluble core material will partially migrate into the vehicle to cause a waste of material or its decomposition may be encouraged by the presence of water. Non-aqueous solvents, which are of necessity limited to certain special high-boiling varieties, cannot be easily removed later.
In the organic solvent method, the separation or evaporation of the solvent is normally carried out in an aqueous phase and, therefore, the method is unsuited for the encapsulation of water-soluble core materials. As a modification of the organic solvent method, there is a process wherein, after dissolution of the encapsulating or shell-forming material in an organic solvent, a non-solvent is added to the solution to depress the solubility in the system until coacervation takes place between the shell-forming material and the solvent, thereby achieving the desired encapsulation. However, the process requires a large quantity of non-solvent and its subsequent recovery presents a major problem.
This invention is characterized in that, while it takes advantage of this phenomenon of coacervation, it does not rely on the use of a non-solvent to accomplish the desired encapsulation but achieves the desired coacervation of the oleaginous component from the solvent by mere temperature adjustment.
Thus, the principal object of the present invention is to provide a novel and industrially feasible method of producing microcapsules. Other objects will be clear from the description and claims hereinafter.
The novel method of the present invention for producing a microencapsulated product, comprises (a) dissolving an oil-and-fat in an organic solvent by heating, said oil-and-fat being solid at room temperature, said organic solvent being hardly or not capable of dissolving a core material to be encapsulated but capable of dissolving said oil-and-fat when hot and capable of coacervating said oil-and-fat when cold, (b) dispersing said core material in the resultant solution, (c) cooling the dispersion with stirring to coacervate the oil-and-fat on the core material, and (d) separating and drying the resultant encapsulated particulate product.
"Oil-and-fat" is mainly composed of glycerin ester of fatty acids (Encyclopedia of Polymer Science and Technology, published by John Wiley & Sons Inc. Vol. 1, 98). The oil-and-fat usable in this invention is solid at room temperature and has a melting point not lower than 30° C., preferably not lower than 50° C., and further preferably not lower than 60° C. The oil-and-fat is exemplified by hydrogenated oil-and-fat (e.g. hydrogenated castor oil, hydrogenated soybean oil, hydrogenated rapeseed oil, hydrogenated beef tallow, hydrogenated palm oil, hydrogenated cottonseed oil, hydrogenated fish oil, hydrogenated whale oil), solid fat (e.g. cacao butter, lard, beef tallow), synthetic solid glyceride (e.g. glycerin monostearate, glycerin distearate, glycerin tristearate) and so on. Among them, hydrogenated oil-and-fat and cacao butter are advantageous, and especially advantageous is hydrogenated oil-and-fat having a melting point not lower than 50° C., preferably not lower than 60° C. such as hydrogenated, castor oil, hydrogenated soybean oil and so on. These materials may be employed alone or as mixture and in the latter case they may be partially replaced by those oils-and-fats which are liquid at room temperature.
The organic solvent may be any appropriate organic solvent, provided that, when hot, it is able to dissolve said oil-and-fat, that the core material to be encapsulated is hardly soluble or insoluble therein and that, when cold, the solvent will coacervate the oil-and-fat to allow the latter to encapsulate the core material. Preferred are the solvents which, when hot, will dissolve not less than 1 percent (weight/volume), desirably not less than 5 percent, of said oil-and-fat and, when cold, will coacervate not less than 50 percent of the dissolved oil-and fat.
Examples of said organic solvents are lower alkanol of up to six carbon atoms (e.g. methanol, ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, n-amyl alcohol, iso-amy alcohol), saturated hydrocarbon (e.g. n-hexane, cyclohexane), ethyl ether, ethylene glycol monomethyl ether, ethyl acetate, acetone, benzene, trichloroethylene and so on. Among them, advantageous are the lower alkanol and the saturated hydrocarbon, especially methanol, ethanol, n-propanol, iso-propanol, n-hexane and cyclohexane. These solvents may be employed alone or as mixture. In mixture, advantageous is a mixture of lower alkanol and saturated hydrocarbon.
Table 1 shows some examples of the preferred combinations of oils-and-fats with solvents.
Table 1______________________________________Combinations of oils-and-fats with solventsOil-and-fat Solvent______________________________________ Methanol Ethanol n-PropanolHydrogenated castor oil iso-Propanol n-Amyl alcohol Ethylene glycol monomethyl ether Ethyl acetate Acetone Benzene n-Hexane Trichloroethylene EtherHydrogenated beef tallow EthanolCacao butter EthanolGlycerin monostearate EthanolMixture of hydrogenated castor oil and hydrogenated Ethanol soybean oil______________________________________
The particulate core material may be whichever of a water-soluble and a water-insoluble material, all that is necessary being that it is solid at room temperature and is either hardly soluble or insoluble in said vehicle. Said core material may have a diameter within the range of 0.1 micron to several millimeters (e.g. 3 millimeters) and, preferably, between 10 microns and 840 microns. These core materials may be any of feed additives, medicines, agricultural chemicals, food additives and so on.
Examples of said core materials are vitamins, minerals, amino acids, antibiotics, synthetic antibacterial or antiprotazoal agents, analgesic antipyretics, enzymes, dried viable microorganisms, feed or food materials, agricultural chemicals and so on. Among them, advantageous are vitamins, antibiotics and enzymes.
Said vitamins are exemplified by thiamine salts and their derivatives (e.g. thiamine mononitrate, thiamine hydrochloride, thiamine tetrahydrofurfuryl disulfide and its hydrochloride, thiamine propyl disulfide and its hydrochloride), pyridoxine hydrochloride, hydroxocobalamine, cyanocobalamine, menadione and its derivatives (e.g. menadione sodium bisulfite, menadione sodium bisulfite complex, menadione dimethylpyrimidinol bisulfite), acetomenaphtone, folic acid, ascorbic acid and its salts (e.g. ascorbic acid, sodium ascorbate, calcium ascorbate), choline chloride, nicotinic acid, nicotinamide and so on.
The minerals are exemplified by potassium iodide, calcium iodate, ferrous sulfate, ferrous fumarate, ferrous threonate and so on.
The amino acids are exemplified by methionine, lysine hydrochloride and so on.
The antibiotics are exemplified by macrolide antibiotics (e.g. oleandomycin, oleandomycin phosphate, triacetyl oleandomycin, kitasamycin, kitasamycin tartrate, kitasamycin succinate, kitasamycin stearate, acetyl kitasamycin, erythromycin, erythromycin ethyl succinate, erythromycin ethyl carbonate, erythromycin stearate, erythromycin propionate, erythromycin propionate lauryl sulfate, T2636 disclosed in Journal of Antibiotics, Vol. 24, No. 1, page 1-12, 1970), tetracyclines (e.g. tetracycline, tetracycline hydrochloride, tetracycline metaphosphate, oxytetracycline, oxytetracycline hydrochloride, ammonium oxytetracyclinate, metacycline hydrochloride, demethyl chlortetracycline, chortetracycline, calcium chlortetracyclinate, chlortetracycline hydrochloride, pyrrolidinomethyltetracycline, tetracycline methylene lysine), penicillins (e.g. sodium penicillin, potassium penicillin, aluminum penicillin, calcium penicillin, benzyl penicillin, benzyl penicillin benzathine, procaine benzyl penicillin, sodium benzyl penicillin, potassium benzyl penicillin, benzyl penicillin aminomethomidine, ampicillin, sodium oxacillin, sodium dicloxacillin, potassium propicillin, phenoxymethyl penicillin benzathine, sodium phenoxymethyl penicillin, calcium phenoxymethyl penicillin, potassium phenoxymethyl penicillin, potassium phenethicillin), cephalosporins (e.g. cephalexin, cephaloglycin), polypeptide antibiotics (e.g. bacitracin, zinc bacitracin, manganese bacitracin, colistin, colistin sulfate, colistin hydrochloride, colistin sodium methanesulfonate, enramycin (enduracidin) hydrochloride, thiopeptin), aminoglycosidic antibiotics (e.g. kanamycin sulfate, fradiomycin sulfate, tobramycin, gentamycin), polyether antibiotics (e.g. T-42082 disclosed in Japanese Patent Publication No. 35494/1976) and other antibiotics (e.g. spiramycin, acetyl spiramycin, spiramycin embonate, chloramphenicol, chloramphenicol parmitinate, chloramphenicol stearoylglycorate, chloramphenicol succinate, chromomycin A3).
The synthetic antibacterial or antiprotozoal agents are exemplified by amprolium, beclotiamine naphthalene-1,5-disulfonate, ethyldimethialium nitrate, dimethialium nitrate, 3-sulfanilamidoisoxazole, 3-sulfanilamidoisoxazole sodium, sulfamethazine, sulfamethazine sodium, sulfamonomethoxine, sulfamonomethoxine sodium, sulfadimethoxine, sulfadimethoxine sodium, sulfaquinoxaline, sulfaquionoxaline sodium, pyrimethamine and so on.
The analgesic antipyretics are exemplified by aspirin, aluminum aspirin and so on.
The enzymes are exemplified by phycomyces lipase, serratia peptidase, aspergillo peptidase, trypsin, diastase, cellulase and so on.
The dried viable microorganisms are exemplified by Streptococcus faecalis, Lactobacillus acidophilus, Lactobacillus salivarus, Lactobacillus bifidus and so on.
The feed or food materials are exemplified by 5'-ribonucleotide, sodium bicarbonate, citric acid, tartaric acid, succinic acid, dried yeast extract and so on.
The agricultural chemicals include pesticides, herbicides, fertilizers or the like, and are exemplified by chlorophenamidine hydrochloride, cartap hydrochloride and so on.
These core materials may be employed alone or as mixture, or may be employed together with a suitable carrier or stabilizer, for example, ascorbic acid-corn starch, menadion dimethylpyrimidinol bisulfite-calcium dihydrogenphosphate and so on.
The dissolution of the oil-and-fat is effected by increasing the temperature of the organic solvent but not to a level as high as to decompose the core material. An advantageous range of the temperature is 50° C. to 100° C. In order to dissolve as much of this shell-forming component as possible, it is recommended that the solvent would be heated to a temperature near its boiling point. The dissolution may be carried out with refluxing the solvent so that the system may be stirred spontaneously. The resultant solution has generally a viscosity lower than 100 centipoises, advantageously lower than 50 centipoises.
The dispersion of the core material to the solution is effected at a temperature higher than the temperature at which the coacervation appears. An advantageous range of the temperature is 30° C. to 100° C., and when the core material which is changeable at a high temperature, for example, enzyme or dried viable microorganism, is employed, advantageous is a temperature not higher than 40° C.
The stirring to be performed at the dispersion step of the core material into the shell-forming material and at the cooling step need not be especially vigorous but, rather, gentle stirring of the order barely enough to preclude a sedimentation or caking of the core material is sufficient. By increasing the stirring speed, the resultant encapsulated products may be obtained in a smaller size. The particle size of the products may be also dependent upon other factors such as the core material, oil-and-fat, etc.
The resultant dispersion is cooled to a temperature within the range from 0° C. to 60° C., advantageously from 20° C. to 45° C. As to the cooling operation, the system may be allowed to cool under room temperature conditions but, to reduce the encapsulation time, forced cooling with water or other cooling medium may also be employed. However, because excessively rapid cooling would cause the shell-forming material to be coacervated in isolation from the core material, it is desirable to reduce the temperature gradually once the system has approached the temperature at which the shell-forming material would start coacervating from the solvent. Generally, the coacervation of an oil-and-fat takes place at a temperature far below the temperature at which it was dissolved. By way of example, hydrogenated castor oil as dissolved in ethanol at 78° C. would start undergoing coacervation in the neighborhood of 50° C. and, as it has been discovered, this coacervation continues for a fairly long time even after the temperature of the system has dropped to room temperature, i.e. 25° to 30° C. Therefore, in order that the oil-and-fat dissolved in a solvent may be allowed to coacervate sufficiently from the solvent, it is necessary that the solution be maintained, under stirring, at the destination temperature of cooling for some time. While the appropriate duration of this time depends upon such variables as the shell-forming material, organic solvent, destination temperature, batch size, etc., it is generally within the range of 10 minutes to 2 hours, advantageously 30 minutes to 2 hours. Where an oil-and-fat melting at 50° C. or less or having high solubility to the solvent is employed as the shell-forming material, no satisfactory coacervation may be obtained at times unless the destination temperature of cooling is held below room temperature. Taking cacao butter as an example, it has been found that the butter separates out from the solvent ethanol when the solution is cooled to a temperature not higher than 5° C.
The encapsulated product can then be separated from the vehicle by a known procedure, exemplified by filtration, centrifugation, adsorption on a suitable particulate solid and so on. From the resultant wet particulate product, the solvent is removed by a procedure known per se at a temperature below the fusing point of the employed oil-and-fat, for example by drying under reduced pressure, in hot air currents or in a fluidized bed or by the spray-drying method, whereby the product can be recovered as independent, free-flowing microcapsules.
In this invention, the ratio of organic solvent to core material is at least 3:1 V/W (not less than 3 ml per gram), advantageously at least 5:1 V/W (not less than 5 ml per gram) and a greater amount of the solvent is necessary where the solubility of the oil-and-fat in the solvent is low. Furthermore, the ratio of the oil-and-fat, which is the shell-forming component, to the core material in the solvent may be optional within the limits of 0.1:1 to 10:1, preferably within the limits of 0.3:1 to 5:1, further preferably wthin the limits of 0.75:1 to 2:1.
In this invention, a polymer may be dissolved in the organic solvent together with the fat-and-oil. The polymer takes a part to support oleocapsule in the encapsulated product under high temperature, for example, a temperature when feed pellet is formed, or a part to make the microcapsule possess a suitable property for sustained release or prolonged action. The polymer is generally dissolved in the organic solvent at a concentration not greater than 5 W/V percent, advantageously at a concentration not greater than 2 W/V percent. In this case, the viscosity of the resultant solution is lower than 100 centipoises, preferably lower than 50 centipoises in the presence of the oil-and-fat. In the above concentration, the polymer itself does not coacervate or precipitate in the system, and, therefore, the polymer in encapsulated product is based upon that dissolved in the solvent which was contained in gel structure of the coacervated oleocapsule. Accordingly, the ratio of the polymer to the oil-and-fat in the resultant oleocapsule is generally not greater than 25 percent by weight basis, advantageously not greater than 10 percent by weight basis. Said polymers are exemplified by cellulose derivatives (e.g. hydroxypropyl cellulose, hydroxypropylmethyl cellulose, cellulose acetate N,N'-di-n-butyl-hydroxypropylether, cellulose acetate phthalate, ethyl cellulose, methyl cellulose), acrylic copolymers (e.g. dimethylaminoethyl methacrylate-methyl methacrylate copolymer, 2-methyl-5-vinylpyridine-methyl acrylatemethacrylic acid copolymer, methacrylate-methacrylic acid copolymer, methyl methacrylate-methacrylic acid copolymer), polyvinylacetal diethylaminoacetate and so on. These materials may be employed alone or as mixture.
In a case that the polymer is employed in this invention, if necessary, a fine powder [e.g. corn starch, lactose, magnesium, stearate, stearate, talc, silicic acid anhydride, SIPERNANT 17 (made by Degussa Co., West Germany)] may be added to the solution after coacervation in order to prevent the adherence among the resultant encapsulated products.
In step (d) of this invention, the resultant dried particulate product may be further mixed with a powdery hydrophobic carrier (e.g. magnesium stearate, aluminum stearate, talc, SIPERNANT 17), heated and then cooled. The heating is carried out at a temperature higher than a melting point of the employed oil-and-fat by degrees not more ten in centigrade. Said temperature is generally from 30° C. to 90° C. and maintained for 10 minutes to 30 minutes. The amount of the powdery hydrophobic carrier, which is employed in order to prevent the adherence among the microencapsulated products at heating, may be generally 0.1 to 5 times of the microencapsulated product by weight basis. The cooling is carried out to a temperature lower than a melting point of the employed oil-and-fat. By this heating and cooling, the density of the oleocapsule is heightened and thereby the oleocapsule wall is strengthened. In this procedure, the oleocapsule which contains the polymer with the oil-and-fat is advantageously employed.
The method according to this invention does not require a non-solvent (a solvent which is otherwise employed to depress the solubility of shell-forming material in a system to cause a coacervation) and requires only a comparatively small amount of a solvent. Moreover, low-boiling alcohols, saturated hydrocarbons and other solvents that are easy to remove later can be successfully employed. Since non-aqueous solvents may also be employed, the method of this invention has the advantage that those kinds of core materials which are readily soluble in water or unstable in the presence of water can also be encapsulated without causing a loss of the ingredients. Moreover, since the coacervation of this invention is caused by only temperature adjustment, this method is very advantageous in industrial applications.
The encapsulated product obtained in the above manner may as such be employed in various applications, e.g. as feed additives, medicines, agricultural chemicals, food additives and so forth, and is excellent in stability of the core material. The encapsulated product may also be diluted with other suitable particulate materials to manufacture powders or processed into tablets or granules together with other suitable compounding ingredients according to appropriate formulas or prescriptions. The microencapsulated product obtained by the foregoing method of this invention may also be used further as a core material for encapsulation by a known method.
The following examples are further illustrative but by no means limitative of this invention.
To 80 ml of ethanol was added 5.0 g of Castor Wax A (Nihon Yushi Ltd., Japan hydrogenated castor oil, melting point 85° C.) and, in a flask fitted with a reflux condenser, the mixture was boiled at 78° C. The resultant solution was transferred to a beaker of stainless steel, to which 5.0 g. of calcium ascorbate (80-200 mesh; Takeda Chemical Industries, Ltd., Japan) was added. Under agitation with a propeller stirrer, the mixture was allowed to cool under room temperature conditions whereby Castor Wax A was caused to coacervate on the calcium ascorbate by way of core material and, thereby, to produce an encapsulated particulate product. This system was centrifuged to remove the ethanol and dried under reduced pressure and at 40° C. for 3 hours. By the above procedure was obtained 9.0 g of calcium ascorbate oleocapsules from 48 to 200 mesh in diameter.
To 1.0 g of Castor Wax A was added 80 ml of n-hexane and, in a flask fitted with a reflux condenser, the mixture was boiled at 69° C. The resultant solution was transferred to a beaker of stainless steel, in which 1.0 g of calcium ascorbate from 80-200 mesh was added. Thereafter, the corresponding procedure of Example 1 was repeated to obtain 1.5 g of calcium ascorbate oleocapsules from 48 to 200 mesh in diameter.
To 1.0 g of hydrogenated beef tallow (Nihon Yushi Ltd., Japan, melting point 45° C.) was added 50 ml of ethanol and, with a reflux condenser, the mixture was boiled at 78° C. The resultant solution was transferred to a beaker of stainless steel, in which 1.0 g of calcium ascorbate from 48-200 mesh was added. Thereafter, the corresponding procedure of Example 1 was repeated to obtain 1.3 g of oleocapsules of calcium ascorbate from 48-200 mesh in diameter. The cooling temperature used, however, was 0° C. in ice-water.
To 2.0 g of cacao butter (Fuji Seiyu Ltd., Japan, melting point 30°-35° C.) was added 80 ml of ethanol and, in a flask fitted with a reflux condenser, the mixture was boiled at 78° C. The resultant solution was transferred to a beaker of stainless steel, in which 2.0 g of calcium ascorbate from 80-200 mesh was added. Under stirring with a propeller stirrer, the mixture was cooled to 0° C., whereby the cacao butter was coacervated on the calcium ascorbate cores to yield an encapsulated product. The system was centrifuged to remove the ethanol and the solid was dried under reduced pressure and at 25° C. for 8 hours. By the above procedure was obtained 3.8 g of calcium ascorbate oleocapsules with diameters in the range of 48 to 200 mesh.
To 2.0 g of glycerin monostearate (Riken Vitamin Oil Ltd., Japan, melting point 58.5°-62.0° C. was added 80 ml of ethanol and, with a reflux condenser, the mixture was boiled at 78° C. The resultant solution was transferred to a beaker of stainless steel, in which 2.0 g of calcium ascorbate from 80-200 mesh was added. Thereafter, the corresponding procedure of Example 1 was repeated to obtain 3.9 g of calcium ascorbate oleocapsules from 48 to 200 mesh in diameter.
5.0 g of Castor Wax A and 5.0 g of soybean oil (The Pharmacopoeia of Japan were taken and 80 ml of ethanol was added. After a reflux condenser was attached, the mixture was boiled at 78° C. The resultant solution was transferred to a beaker of stainless steel, in which 5.0 g of calcium ascorbate from 80 to 200 mesh was added. Thereafter, the corresponding procedure of Example 1 was repeated to obtain 13.4 g of calcium ascorbate oleocapsules from 48 to 200 mesh in diameter.
The procedure of Example 1 was repeated except that 5.0 g of dry iron sulfate not exceeding 200 mesh (The Pharmacopoeia of Japan) was used in lieu of calcium ascorbate. By this procedure was obtained 8.8 g of oleocapsules of dry iron sulfate from 32 to 100 mesh in diameter.
The procedure of Example 1 was repeated except that 1.0 g of aluminum aspirin (average diam. about 5 μ) was used in lieu of calcium ascorbate to obtain 4.7 g of aluminum aspirin oleocapsules from 60 to 100 mesh in diameter.
To 2.0 g of Castor Wax A was added a mixture of 40 ml ethanol and 40 ml n-hexane and, with a reflux condenser, the system was heated at 70° C. The resultant solution was transferred to a beaker of stainless steel, in which 2.0 g of calcium ascorbate, 80 to 200 mesh, was added. Thereafter, the corresponding procedure of Example 1 was repeated to obtain 3.8 g of calcium ascorbate oleocapsules from 48 to 200 mesh in diameter.
(1) Producing Procedure
A. To a solid oil-and-fat was added a solvent or a mixture of solvents and, with a reflux condenser, the system was heated at a temperature near the boiling point of the solvent. The resultant solution was transferred to a beaker of stainless steel, to which a core material was added. Under agitation with a propeller stirrer, the mixture was allowed to cool under room temperature conditions, if necessary with making use of ice, whereby the oil-and-fat was coacervated around the core material and, thereby, to produce an encapsulated particulate product. This system was filtrated or centrifuged to remove the solvent and dried under reduced pressure and at room temperature for 16 hours.
B. To a solid oil-and-fat and polymer was added a solvent or a mixture of solvents and, with a reflux condenser, and processed in the same manner as in Procedure A. After coacervation, if necessary fine powders such as Corn starch, Lactose, etc. were added to the solvent to prevent the microcapsules from the adhesion of particles.
The formulation, producing condition, and the yield and particle size of the resultant microcapsules are shown in Table 2.
Table 2__________________________________________________________________________ Temperature of dispers- Fine powderExample solid oil- ing core Microcapsule dispersedNo. Core material and-fat Polymer Solvent material Yield Particle size Procedure in__________________________________________________________________________ solventSodium ascor- Castor Wax n-hexanebate(100-200 A(Nihon ;80ml10 mesh;Takeda Yushi Ltd., None n- 53° C. 1.29g 16-100mesh A NoneChemical Japan, propanolIndustries, hydroge- ;5mlLtd.,Japan) nated; 1 g castor oil, m.p. 85° C.); 2g n-hexane ;400ml11 "; "; None iso- 60°C. 9.38g 16-80mesh A None5g 10g propanol ;25ml Ethocel12 "; "; STD3) " 52° C. 10.17g 16-120mesh B None5g 10g ;3.5g L.B.Wax1) ethanol;13 "; (Nihon Yushi None 80ml 61° C. 1.52g 16-100mesh A None1g Ltd., Japan m.p. 60° C.) ;2g Lubri Wax 1022)14 "; (Freund Ind. None n-hexane 52° C. 2.38g 32-100mesh A None1g Co.,Ltd. ;80ml Japan,m.p. 62° C.);2g hydroge- nated beef tallow15 "; (Nihon Yushi None ethanol 65° C. 117.5g 32-100mesh A None50g Ltd. Japan, ;1200ml m.p.60° C.); 100g Castor Wax n-hexane A;50g ;1200ml16 "; None trichlo- 70° C. 82.1g 16-100mesh A None50g roethy- lene ;50ml17 "; "; None " 70° C. 125.1g 16-100mesh A None50g 100g Ethocel n-hexane 60° C. 22.5g 32-100mesh B corn18 "; "; STD ;800ml starch10g 20g ;3g n- :5g propanol ;50mlascorbic acid n-hexane(100-200mesh; ;80 mlTakeda n-19 Chemical " ; HPC-L4) propanol 60° C. 1.8g 16-60mesh B NoneIndustries 2g ;0.7g ;5 mlLtd.,Japan) ethanol;1g ;1Omlmenadione Castor n-hexanedimethyl- Wax A ;80mlpyrimidinol ;2g trichlo-20 bisulfite ( None roethy- 52° C. 2.0g 32-100mesh A None100-200mesh) lene;1g ;5ml n-hexane ;80ml Ethocel trichlo-21 "; "; STD roethy- 54° C. 2.0g " B None1g 2g ;0.7g lene ;5ml n- propanol ;5mlmenadione Castor Ethocel n-hexanedimethyl- Wax A STD ;80mlpyrimidinol ;2g ;0.7g tri-bisulfite( chloro-22 100-200mesh) ethylene 53° C. 1.8g 32-100mesh B None;1g ;5ml iso- propanol ;5ml23 "; Lubri Wax None n-hexane 52° C. 2.2g " A None1g 102;2g ;80ml24 "; "; CAP5) acetone 52° C. 2.1g 32-100mesh B None1g 2g ;0.7g ;80ml25 "; L.B.Wax;2g None ethanol 61° C. 1.3g 16-200mesh A None1g ;80mlmenadione Castor n-hexanesodium Wax A;2g ;80ml26 bisulfite None 52° C. 1.7g 16-100mesh A None(200-300mesh) n-;1g propanol ;5ml27 "; L.B.Wax;2g None iso- 66° C. 1.3g 32-200mesh A None1g propanol ;80mlmenadione Castor n-hexanedimethyl- Wax A ;80ml28 pyrinidinol ;2g None n- 53° C. 1.5g 32-100mesh A Nonebisulfite propanol(100-200 ;5mlmesh);1gfolic acid Castor n-hexane29 (100-200mesh) Wax A None ;80ml;1g ;2g n- 53° C. 2.2g 16-60mesh A None propanol ;5ml Ethocel n-hexane STD ;80ml Lactose;1g30 "; "; ;0.7g ethanol 52°C. C 3.1g " B1g 2g ;10ml Lubri n-hexane31 Wax 102 ;80ml"; ;2g None iso- 52° C. 1.8g " A None1g propanol ;5ml hydro- genated32 "; beef tallow None n-hexane 52° C 1.3g 32-200mesh A None0.2g ;2g ;80mlfolic acid L.B.Wax None n-hexane 53° C. 1.2g 32-200mesh A None33 (100-200mesh) ;2g ;80ml0.2gthiamine Castor n-hexane;34 mononitrate Wax A;2g None 80ml 52° C. 1.3g 16-200mesh A None(200-300mesh) iso-;1g propanol ;5mlthiamine Castor35 tetrahydro- Wax A;2g None " " 1.2g 16-60mesh A Nonefurfuryldisulfide(60-200mesh);1gpyridoxine36 hydrochloride " None " " 1.4g " A None(60-200mesh);1gcyano-37 cobalamin " None " " 1.1g " A None(200-300mesh);1gcholine Castor n-hexanechloride Wax A ;80ml38 (16-32mesh) ;2g iso- 53° C. 0.8g 9-32mesh A None;1g propanol ;5mlDL-methionine39 (60-200mesh) " None " 51° C. 1.6g 16-60mesh A None;1gL-lysine40 hydrochloride " None " 53° C. 1.3g 16-80mesh A None(60-200mesh);1gcalcium41 iodate(100- " None " 52° C. 1.0g 16-60mesh A None300mesh);1g5'-ribo-42 nucleotide " None " 51° C. 0.8g 16-100mesh A None(60-200mesh);1gChloro- Castor n-hexanephenamidine Wax A;2g ;80ml43 hydro- None iso- 52°C. 1.4g 16-60mesh A Nonechloride(32- propanol-100mesh);1g ;5mlCartaphydro-44 chloride(200-"; None " 52° C. 1.1g " A None300 mesh);1g 2g n-hexane ;80ml45 T-26366) ;1g "; None n- 52° C. 1.6g 16-60mesh A None 2g propanol ;5mltriacetyl- n-hexaneoleandomycin ;80ml46 (60-200mesh) "; None iso- 52° C. 1.2g " A None;1g 2g propanol ;5mltetracycline Lubri Wax None n-hexane 52° C. 1.3g " A None47 (200-300mesh) 102;2g ;80ml;1gchlortetra- Castor n-hexanecycline Wax A;2g ;80ml48 hydrochloride None n- 52° C. 1.6g 16-60mesh A None(200-300mesh) propanol;1g ;5mlethyl- n-hexanedimethialium Castor ;80ml49 nitrate(200- Wax A;2g None iso- 52° C. 1.0g 32-200mesh A None300 mesh; propanolTakeda ;5mlChemicalInd.Ltd.);1gPhycomyces Castor n-hexane50 Lipase(200- Wax A;2g None ;80ml 52° C. 2.3g 32-100mesh A None300mesh,TakedaChemical Ind.Ltd.,Japan);1g51 "; L.B.Wax;2g None n-hexane 35° C. 2.3g 60-120mesh A None1g ;80ml__________________________________________________________________________
1. hydrogenated castor oil plus hydrogenated soybean oil
2. hydrogenated soybean oil
3. ethyl cellulose (Dow Chem. Co. U.S.A.)
4. hydroxy propyl cellulose (Nihon Soda Ltd., Japan)
5. cellulose acetate phthalate
6. Journal of Antibiotics, Vol. 24, No. 1, page 1-12, 1970
To 0.4 g of the sodium ascorbate oleocapsules obtained according to Example 12 was added 1.2 g of magnesium stearate as a carrier and mixed well. The mixture was heated at 90° C. for 30 minutes and allowed to cool under room temperature conditions, and 50 ml of water and 0.5 ml of 1% starch solution were added. Under agitation with a magnetic stirrer, 0.1N-iodine reagent was added dropwise to determine the percent dissolution of sodium ascorbate into water by plotting the cumulative consumption of iodine on a time axis. The sodium ascorbate oleocapsules obtained according to Example 12 were run as reference control. The results are set forth in Table 3, which shows that the oleocapsules are strengthened by the above treatment, and thereby the dissolution of sodium ascorbate is significantly retarded.
Table 3______________________________________Percent dissolution of sodium ascorbate into waterTest Time (min.)material 5 10 20______________________________________Sodium ascorlateoleocapsules(Example 12)control 45 70 88Sodium ascorbateoleocapsules(Example 52) 9 16 26______________________________________
About 400 mg of the calcium ascorbate oleocapsules obtained according to Example 1 were accurately weighed and 50 ml of water and 0.5 ml of 1% starch solution were added. Under agitation with a magnetic stirrer, 0.1N-iodine reagent was added dropwise to determine the percent dissolution of calcium ascorbate into water by plotting the cumulative consumption of iodine on a time axis. Calcium ascorbate in the sizes of 80 to 200 mesh was run as reference control. The results are set forth in Table 4, which shows that the encapsulation significantly retards the dissolution of calcium ascorbate.
Table 4______________________________________Percent dissolution of calcium ascorbate into waterTest Time (min.)material 1 2 10 20 30 40 50 60______________________________________Calciumascorbate80-200 mesh(control) 99.9 100.0 100.0 -- -- -- -- --Calciumascorbateoleocap-sules,48-200 mesh 0.6 1.3 9.2 19.4 27.7 35.6 43.0 51.3______________________________________48-200 mesh
To "Premix for fish feed" shown in Table 5 was added sodium ascorbate oleocapsule of Example 17 or sodium ascorbate as a control so as to make its concentration 5% and, enclosed in a bag of polyethylene and stored under the room temperature conditions in summer in Japan for 12, 21, and 31 days and tested on their stabilities. They were assayed by indophenol colorimetric method.
The results were shown in Table 6.
Table 5______________________________________Formulation of Premix for fish feed (per kg)Retinol 6670000I.U.Cholecalciferol 1670000I.U.α-tocopherol 26700I.U.Menadione 0.667 gThiamine Mononitrate 5.0 gRiboflavine 10.0 gPyridoxine hydrochloride 4.0 gNicotinamide 26.7 gCalcium pantothenate 20.0 gCholine chloride 200.0 gFolic acid 1.34 gCyanocobalamine 3.34 mgInositol 23.4 gBiotin 0.0667 gManganese sulfate 10.0 g (as Mn)Iron fumarate 16.7 g (as Fe)Cupric sulfate 3.34 g (as Cu)Zinc sulfate 10.0 g (as Zn)Calcium iodate 0.167 g (as I2)Solvent extracted rice bran q.s.______________________________________
Table 6______________________________________Stability of sodium ascorbate in Premix 12 21 31 Initial days days days______________________________________Sodium ascorbate mg/goleocapsule 50.7 48.7 48.7 48.2(Example 17) (100) (96) (96) (95)Sodium ascorbate mg/g(200 Mesh pass) 48.2 1.0 0.5 0.3 (100) (2) (1) (1)______________________________________ (): residual percent
To the broiler premix shown in Table 7 was added menadion dimethylpyrimidinol bisulfite (MPB) oleocapsules of Example 20 or 21, or MPB as a control so as to make its concentration 1.00 mg/g and, stored in a glass bottle at 40° C. for 2 weeks.
They were assayed by gas chromatographic method described in Journal of Association of Official Analytical Chemists, Vol. 56, 1277-1280 W-victor et al. The results were shown in Table 8.
Table 7______________________________________Formulation of broiler premixIngredients Amounts (per Kg)______________________________________Rovimix AD3 500/100** V.A.*; 3000000I.U. V.D3 *; 600000I.U.Rovimix E-50** V.E.*; 3.0 gThiamine mononitrate 0.2 gRiboflavine 3.0 gPyridoxine hydrochloride 1.0 gCyanocobalamine 0.0025 gCalcium panthothenate 2.0 gNicotinamide 5.0 gCholine chloride 120.0 gFolic acid 0.1 gFerrous sulfate Fe; 30.0 gCupric sulfate Cu; 3.8 gManganese sulfate Mn; 25.0 gZinc sulfate Zn; 25.0 gCobaltous sulfate Co; 0.024 gSolvent extracted rice bran added to make 1000 g______________________________________ *V.A retinol V.D.3 cholecalciferol V.E.α-tocopherol **produced by Hoffman La Roche Co.
Table 8______________________________________Stability of MPB in broiler premix Initial 40° C., 2 weeks______________________________________MPBoleocapsules; 1.02 mg/g 1.03 mg/g (101%)Example 20MPBoleocapsules; 1.01 mg/g 0.99 mg/g (98%)example 21MPB(100-200 mesh) 0.92 mg/g 0.54 mg/g (59%)______________________________________ () residual percent
Phycomyces Lipase oleocapsules of Examples 50 and 51 were tested on their enzymatic stabilities in the process of the encapsulation. Lipase activity was assayed by the method described in Journal of The Takeda Research Laboratries, Vol. 35, 1-10, Tomoda et al.
The reaction mixture containing 5 ml of 25% olive oil emulsified with poly-vinyl alcohol, 4 ml of 0.1M phosphate buffer, pH 7.0 and 1 ml of enzyme solution*, was incubated at 37° C. for 50 min. in the Monod shaker. Enzyme reaction was terminated with the addition of 20 ml of acetone : ethanol mixture (1:1 V/V). An amount of liberated fatty acid was titrated with 0.05N NaOH with phenolphthalein as an indicator. One unit of lipase activity was defined as the amount which liberated 1μ mole of free fatty acid per min. at the conditions mentioned above.
The results were shown in Table 9. The loss of enzyme activity in the process of the encapsulation was less than 10%.
Table 9______________________________________Stability of Phycomyces Lipase oleocapsules in theprocess of their productions Lipase activitySample (U/mg) Specific activity**______________________________________Phycomyces Lipase 140 66 (100)Phycomyces Lipaseoleocapsules;Example 50 57 62 (94)Phycomyces Lipaseoleocapsules;Example 51 53 60 (91)______________________________________ (): Index of specific activity **: Lipase activity per absorbance 1.000 at 280 nm corresponding to a uni amount of the protein.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2805977 *||Jan 4, 1955||Sep 10, 1957||Smith Kline French Lab||Sustained release pharmaceutical preparation|
|US2875130 *||Nov 20, 1956||Feb 24, 1959||Smith Kline French Lab||Method of preparing sustained release particles and the product of the method|
|US2967177 *||Mar 31, 1958||Jan 3, 1961||Bristol Myers Co||Process of antibiotic purification|
|US3082154 *||Apr 12, 1961||Mar 19, 1963||Ici Ltd||Improved free-flowing coated antimalarial salts in particulate form|
|US3196018 *||Aug 8, 1960||Jul 20, 1965||Galler William||Coated menadione bisulfite adduct|
|US3415758 *||May 3, 1962||Dec 10, 1968||Ncr Co||Process of forming minute capsules en masse|
|US3541204 *||Dec 2, 1968||Nov 17, 1970||Sibbald Ian Ramsay||Encapsulated biologically active materials for feeding to ruminants and process for the production thereof|
|US3584114 *||May 22, 1968||Jun 8, 1971||Hoffmann La Roche||Free-flowing powders|
|US3960757 *||Jun 29, 1973||Jun 1, 1976||Toyo Jozo Co., Ltd.||Process for encapsulation of medicaments|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4332790 *||Nov 23, 1979||Jun 1, 1982||Societe D'assistance Technique Pour Produits Nestle S.A.||Microcapsule containing a microorganism and a process for its production|
|US4379038 *||Sep 19, 1980||Apr 5, 1983||Japan Atomic Energy Research Institute||Process for preparing a physiologically active substance controlled release composite composition|
|US4380534 *||Apr 1, 1981||Apr 19, 1983||Yamanouchi Pharmaceutical Co., Ltd.||Solid drug preparations|
|US4460563 *||Apr 2, 1981||Jul 17, 1984||Eurand S.P.A.||Process for preparing microcapsules in a liquid vehicle|
|US4525339 *||Oct 15, 1982||Jun 25, 1985||Hoffmann-La Roche Inc.||Enteric coated oral dosage form|
|US4568745 *||Jun 22, 1983||Feb 4, 1986||Luigi Stoppani S.P.A.||Adduct of mutually stabilizing menadione and thiamine|
|US4597960 *||Jun 3, 1983||Jul 1, 1986||Cohen Edgar C||Microencapsulated astringent hemostatic agents and methods of use|
|US4605550 *||Jun 5, 1984||Aug 12, 1986||A. H. Robins Company, Inc.||Delayed release formulations and processes for making them|
|US4675236 *||Oct 30, 1985||Jun 23, 1987||Ohkawara Kokohki Co., Ltd.||Mono-core type microcapsules and process for producing them|
|US4713245 *||May 24, 1985||Dec 15, 1987||Mitsui Toatsu Chemicals, Incorporated||Granule containing physiologically-active substance, method for preparing same and use thereof|
|US4749575 *||Jan 29, 1986||Jun 7, 1988||Bio-Dar Ltd.||Microencapsulated medicament in sweet matrix|
|US4761407 *||Oct 22, 1985||Aug 2, 1988||Rhone-Poulenc Sante||Solid galenical form for oral administration, and the process for its preparation|
|US4818521 *||Nov 24, 1986||Apr 4, 1989||Sunstar Kabushiki Kaisha||Emulsion cosmetic stably containing vitamin C|
|US4829057 *||May 13, 1988||May 9, 1989||R. P. Scherer Corporation||Oxytetracycline capsules with increased stability and methds of producing the same|
|US4844896 *||Nov 2, 1987||Jul 4, 1989||Lim Technology Laboratories, Inc.||Microencapsulated insecticidal pathogens|
|US4884873 *||Oct 27, 1987||Dec 5, 1989||Manchester R & D Partnership||Encapsulated liquid crystal material, apparatus and method having interconnected capsules|
|US4943449 *||Sep 1, 1987||Jul 24, 1990||Ohkawara Kakohki Co., Ltd.||Microcapsules and process for producing them|
|US4948586 *||Aug 18, 1988||Aug 14, 1990||Lim Technology Laboratories, Inc.||Microencapsulated insecticidal pathogens|
|US5000958 *||Jul 26, 1984||Mar 19, 1991||The Liposome Company, Inc.||Enhancement of pharmaceutical activity|
|US5013868 *||Jan 13, 1988||May 7, 1991||Lejus Medical Aktiebolag||Process for treating amphoteric amino acids|
|US5082351 *||Apr 14, 1989||Jan 21, 1992||Manchester R & D Partnership||Encapsulated liquid crystal material, apparatus and method|
|US5089904 *||Oct 31, 1990||Feb 18, 1992||Fergason James L||Encapsulated liquid crystal material, apparatus and method|
|US5188851 *||Nov 20, 1990||Feb 23, 1993||Sanyo-Kokusaku Pulp Co., Ltd.||Feed composition for fish breeding including mononucleotides|
|US5578580 *||Nov 20, 1995||Nov 26, 1996||Ascor Chimici S.R.L.||Veterinary composition, feedstuff and process|
|US5589194 *||Sep 20, 1993||Dec 31, 1996||Minnesota Mining And Manufacturing Company||Method of encapsulation and microcapsules produced thereby|
|US5741478 *||Nov 15, 1995||Apr 21, 1998||Andaris Limited||Preparation of hollow microcapsules by spray-drying an aqueous solution of a wall-forming material and a water-miscible solvent|
|US5891476 *||Dec 22, 1997||Apr 6, 1999||Reo; Joe P.||Tastemasked pharmaceutical system|
|US5957848 *||Jun 5, 1995||Sep 28, 1999||Andaris Limited||Preparation of further diagnostic agents|
|US6015546 *||Jun 5, 1995||Jan 18, 2000||Quadrant Healthcare (Uk) Limited||Preparation of further diagnostic agents|
|US6017310 *||Oct 4, 1996||Jan 25, 2000||Andaris Limited||Use of hollow microcapsules|
|US6022525 *||Aug 22, 1995||Feb 8, 2000||Quadrant Healthcare (Uk) Limited||Preparation of diagnostic agents|
|US6068600 *||Dec 6, 1996||May 30, 2000||Quadrant Healthcare (Uk) Limited||Use of hollow microcapsules|
|US6080428 *||Jan 14, 1995||Jun 27, 2000||Bova; David J.||Nicotinic acid compositions for treating hyperlipidemia and related methods therefor|
|US6129930 *||Mar 6, 1997||Oct 10, 2000||Bova; David J.||Methods and sustained release nicotinic acid compositions for treating hyperlipidemia at night|
|US6132769 *||Mar 20, 1996||Oct 17, 2000||Universiteit Gent||Pharmaceutical matrix pellets, tablets and composition for the preparation thereof|
|US6242019 *||Jul 30, 1998||Jun 5, 2001||Warner-Lambert Company||Taste modified hard confectionery compositions containing functional ingredients|
|US6344182||Oct 8, 1993||Feb 5, 2002||Quadrant Healthcare (Uk) Limited||Preparation of diagnostic agents by spray drying|
|US6348186||Jun 5, 1995||Feb 19, 2002||Quadrant Healthcare (Uk) Limited||Preparation of further diagnostic agents|
|US6416741||Sep 3, 1999||Jul 9, 2002||Quadrant Healthcare (Uk) Limited||Preparation of further diagnostic agents|
|US6569405||Sep 28, 1999||May 27, 2003||Quadrant Healthcare (Uk) Limited||Preparation of diagnostic agents|
|US6576264||Oct 17, 1996||Jun 10, 2003||Skyepharma Canada Inc.||Insoluble drug delivery|
|US6623722||Feb 13, 1998||Sep 23, 2003||Quadrant Healthcare (Uk) Limited||Spray-drying microcapsules using an aqueous liquid containing a volatile liquid|
|US6634576||Aug 29, 2001||Oct 21, 2003||Rtp Pharma Inc.||Milled particles|
|US6676967||Oct 31, 1997||Jan 13, 2004||Kos Pharmaceuticals, Inc.||Methods for reducing flushing in individuals being treated with nicotinic acid for hyperlipidemia|
|US6682761||Apr 20, 2001||Jan 27, 2004||Rtp Pharma, Inc.||Water-insoluble drug particle process|
|US6746691||Oct 31, 1997||Jun 8, 2004||Kos Pharmaceuticals, Inc.||Intermediate release nicotinic acid compositions for treating hyperlipidemia having unique biopharmaceutical characteristics|
|US6773733 *||Mar 26, 2001||Aug 10, 2004||Loders Croklaan Usa Llc||Structured particulate systems|
|US6818229||Oct 31, 1997||Nov 16, 2004||Kos Pharmaceuticals, Inc.||Intermediate release nicotinic acid compositions for treating hyperlipidemia|
|US6939530||Jun 21, 2002||Sep 6, 2005||Quadrant Drug Delivery Limited||Preparation of further diagnostic agents|
|US6974593||Jun 9, 2003||Dec 13, 2005||Jagotec Ag||Insoluble drug delivery|
|US6979456||Mar 30, 1999||Dec 27, 2005||Jagotec Ag||Anticancer compositions|
|US7041705||Mar 26, 2001||May 9, 2006||Jagotec Ag||Injectable aqueous dispersions of propofol|
|US7097849||Aug 18, 1999||Aug 29, 2006||Jagotec Ag||Injectable aqueous dispersions of propofol|
|US7255877||Mar 31, 1999||Aug 14, 2007||Jagotec Ag||Fenofibrate microparticles|
|US7939105||Nov 19, 1999||May 10, 2011||Jagotec Ag||Process for preparing a rapidly dispersing solid drug dosage form|
|US7939106||May 23, 2003||May 10, 2011||Jagotec Ag||Process for preparing a rapidly dispersing solid drug dosage form|
|US7998506||Aug 16, 2011||Kos Life Sciences, Inc.||Nicotinic acid compositions for treating hyperlipidemia and related methods therefor|
|US8206746||Sep 30, 2002||Jun 26, 2012||Jagotec Ag||Microparticles of water-insoluble substances|
|US8415329||Apr 9, 2013||Jagotec Ag||Thermoprotected compositions and process for terminal steam sterilization of microparticle preparations|
|US8586094||May 2, 2003||Nov 19, 2013||Jagotec Ag||Coated tablets|
|US8703202||Jul 24, 2006||Apr 22, 2014||Jagotec Ag||Coated tablets|
|US9149567||Mar 9, 2010||Oct 6, 2015||Ansell Limited||Powder-free antimicrobial coated glove|
|US9186640||Aug 28, 2007||Nov 17, 2015||Pepsico, Inc.||Delivery and controlled release of encapsulated lipophilic nutrients|
|US20020119199 *||Mar 31, 1999||Aug 29, 2002||Indu Parikh||Fenofibrate microparticles|
|US20030013693 *||Apr 22, 2002||Jan 16, 2003||Rtp Pharma Inc.||Method and composition for treatment of inflammatory conditions|
|US20030133876 *||Jun 21, 2002||Jul 17, 2003||Quadrant Healthcare (Uk) Limited, A Member Of The Elam Group Of Companies||Preparation of further diagnostic agents|
|US20030232091 *||Jun 17, 2002||Dec 18, 2003||Adi Shefer||Stabilized retinol for cosmetic dermatological, and pharmaceutical compositions, and use thereof|
|US20040018229 *||Jun 9, 2003||Jan 29, 2004||Henriksen Inge B.||Insoluble drug delivery|
|US20040086571 *||Mar 17, 2003||May 6, 2004||Skyepharma Canada Inc.||Fibrate-statin combinations with reduced fed-fasted effects|
|US20050003070 *||Jul 3, 2003||Jan 6, 2005||Foster David V.||Shelf stable vitamin C in oatmeal products|
|US20050118257 *||May 23, 2003||Jun 2, 2005||Bova David J.||Nicotinic acid compositions for treating hyperlipidemia and related methods therefor|
|US20050238586 *||Jun 23, 2005||Oct 27, 2005||Quadrant Drug Delivery Limited||Preparation of further diagnostic agents|
|US20060210622 *||Nov 14, 2005||Sep 21, 2006||Skyepharma Canada Inc.||Surface modified particulate compositions of biologically active substances|
|US20080045573 *||Aug 15, 2007||Feb 21, 2008||Bova David J||Methods and Sustained Release Nicotinic Acid Compositions for Treating Hyperlipidemia|
|US20090061048 *||Aug 28, 2007||Mar 5, 2009||Pepsico, Inc.||Delivery and controlled release of encapsulated lipophilic nutrients|
|US20090169677 *||Jun 16, 2006||Jul 2, 2009||Helle Wittorff||Chewing Gum Comprising a Hydrophobic Enzyme Formulation|
|US20100229282 *||Sep 16, 2010||Ansell Limited||Powder-Free Anti-Blocking Coated Glove|
|US20100233223 *||Sep 16, 2010||Ansell Limited||Powder-Free Antimicrobial Coated Glove|
|US20100272859 *||Oct 28, 2010||Pepsico, Inc.||Delivery and controlled release of encapsulated water-insoluble flavorants|
|USRE40059||Nov 29, 2001||Feb 12, 2008||Balchem Corporation||Sensitive substance encapsulation|
|EP0037740A2 *||Apr 7, 1981||Oct 14, 1981||Yamanouchi Pharmaceutical Co. Ltd.||Solid microdose drug preparation|
|EP0038585A1 *||Mar 31, 1981||Oct 28, 1981||EURAND ITALIA S.p.A.||Process for preparing microcapsules in a liquid vehicle|
|EP0079668A1 *||Aug 27, 1982||May 25, 1983||Sierra Chemical Company||Pesticide product and use and manufacture thereof|
|EP0380225A2 *||Jan 16, 1990||Aug 1, 1990||Pfizer Inc.||Low calorie fat substitute|
|EP0411326A2 *||Jun 29, 1990||Feb 6, 1991||Bio-Dar Ltd.||Microcapsules containing food additives and their use|
|EP1433525A1 *||Dec 13, 2000||Jun 30, 2004||Balchem Corporation||Sensitive substance encapsulation|
|WO1985000515A1 *||Jul 27, 1984||Feb 14, 1985||The Liposome Company, Inc.||Enhancement of antimicrobial activity by incorporating mixture of antimicrobial agents into lipid vesicles|
|WO1990009108A1 *||Jan 25, 1990||Aug 23, 1990||Wm. Wrigley Jr. Company||Enhanced food vitamin addition by microbead delivery|
|WO1994009636A1 *||Oct 21, 1993||May 11, 1994||Mars, Inc.||Competitive organism preservation|
|WO1996003041A1 *||Jul 12, 1995||Feb 8, 1996||Ciba-Geigy Ag||Spherical microparticles having an inner wax coating deposited around biologically active compounds|
|WO2005067730A1 *||Jan 19, 2005||Jul 28, 2005||Dr. Paul Lohmann Gmbh Kg||Method for the production of microencapsulated particles containing iron-ii-sulphate|
|U.S. Classification||428/402.2, 514/562, 424/94.3, 424/648, 514/159, 426/805, 424/419, 424/93.1, 426/72, 435/177, 514/276, 424/646, 514/474, 514/152, 427/213.3, 428/402.24, 514/345, 424/639, 514/249, 424/668, 71/64.11, 424/641, 264/4.4, 424/637, 514/29, 424/497, 514/682|
|International Classification||A61K9/50, A23K1/00, C05G3/00, A01N25/28, B01J13/10, B01J13/08, A23L1/00|
|Cooperative Classification||Y10T428/2989, Y10T428/2984, B01J13/10, C05G3/0017, A23K1/004, A01N25/28, A23L1/0032, A61K9/50, Y10S426/805|
|European Classification||A23L1/00P4B, A61K9/50, A23K1/00B3, B01J13/10, C05G3/00B2D, A01N25/28|